| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30067017-30067325 | Common:3; Rare:57 | ||||
| chr6:30213356-30213578 | Common:2; Rare:57 | ||||
| chr6:30326360-30326534 | Common:1; Rare:31 | ||||
| chr6:30326832-30326939 | Rare:32 | ||||
| chr6:30555821-30556381 | Common:1; Rare:163 | ||||
| chr6:30556383-30556712 | Common:1; Rare:76 | ||||
| chr6:30557210-30557342 | Common:1; Rare:49 | ||||
| chr6:30571246-30571503 | Common:1; Rare:88 | ||||
| chr6:30686638-30686779 | Common:1; Rare:27 | ||||
| chr6:30687150-30687410 | Rare:54 | ||||
| chr6:30717259-30717435 | Common:1; Rare:37 | ||||
| chr6:30742504-30743063 | Common:2; Rare:119 | ||||
| chr6:30744288-30744381 | Rare:23 | ||||
| chr6:30882733-30882982 | Common:2; Rare:30 | ||||
| chr6:30914017-30914377 | Common:2; Rare:111; Clinvar (benign):2 |